Homo sapiens solute carrier family 13 member 3 (SLC13A3), transcript v - Nucleotide

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Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability. [BMC Neurol. 2023]
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.
Hussain SI, Muhammad N, Shah SUD, Fardous F, Khan SA, Khan N, Rehman AU, Siddique M, Wasan SA, Niaz R, et al. BMC Neurol. 2023 Oct 4; 23(1):353. Epub 2023 Oct 4.
Sequential genome-wide CRISPR-Cas9 screens identify genes regulating cell-surface expression of tetraspanins. [Cell Rep. 2023]
Sequential genome-wide CRISPR-Cas9 screens identify genes regulating cell-surface expression of tetraspanins.
Yang J, Guo F, Chin HS, Chen GB, Ang CH, Lin Q, Hong W, Fu NY. Cell Rep. 2023 Feb 28; 42(2):112065. Epub 2023 Jan 31.
Association of Single Nucleotide Polymorphisms in KCNA10 and SLC13A3 Genes with the Susceptibility to Chronic Kidney Disease of Unknown Etiology in Central Indian Patients. [Biochem Genet. 2023]
Association of Single Nucleotide Polymorphisms in KCNA10 and SLC13A3 Genes with the Susceptibility to Chronic Kidney Disease of Unknown Etiology in Central Indian Patients.
Kumari R, Tiwari S, Atlani M, Anirudhan A, Goel SK, Kumar A. Biochem Genet. 2023 Aug; 61(4):1548-1566. Epub 2023 Jan 25.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the SLC13A3 gene.
RefSeq protein product
See the reference protein sequence for Na(+)/dicarboxylate cotransporter 3 isoform e (NP_001180271.1).

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Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Nucleotide